[新皮肤试验diaskintest®诊断儿童和青少年结核感染的敏感性]。

Pub Date : 2010-01-01
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引用次数: 0

摘要

在俄罗斯,已经设计了一种皮内药物Diaskintest®,这是一种重组结核病过敏原,基于结核杆菌特异性蛋白:ESAT-6和CFP-10,由转基因大肠杆菌培养产生。对300名患有结核病的儿童和青少年同时进行Diaskintest®试验和Mantoux试验(2TE PPD-L),并在结核病药房对危险人群进行随访,以确定新皮肤试验对活动性结核病感染的敏感性。Diaskintest®不仅对活动性肺结核,而且对隐匿性肺结核感染也有很高的敏感性。以下证据表明了这一点。在接受强化化疗的儿童和青少年结核病患者中,对Diaskintest®的阳性反应比例很高(83.8%)。在分解阶段只观察到少量的阴性试验。在完成治疗的儿童中,78.3%的检测结果呈阳性,而且在先前有胸内淋巴结结核的儿童中也是如此;在治疗开始后不早于18个月观察到阴性试验。Diaskintest®在早期原发性结核感染儿童和与细菌排泄者有家庭接触的儿童中敏感性最高(91.7%)。这些儿童可能被判断为具有潜伏性结核感染的最高保证,在研究时,其人口处于活跃状态。早期原发性结核感染的儿童,但没有家庭接触细菌排泄个体,在治疗前(37.5%)和治疗后(10%)对Diaskintest®的阳性反应百分比较低,这表明儿童的细菌负担一定较低。在对结核菌素有过敏反应的受试者中,对Diaskintest®的阳性反应比例很高(76.2%)。在接受预防性治疗的患者中,这一比例仅为16.7%。在Mantoux试验持续阳性(超过3年)的儿童和青少年中,大多数病例对Diaskintest®的反应为阴性,因为在分枝杆菌传播的早期感染中,对药物的反应是阳性的,但随着3年的过去,感染过渡到持续阶段的可能性很高,此时对Diaskintest®的反应变为阴性。Diaskintest®不会引起与卡介苗接种相关的迟发性超敏反应,表明其具有高特异性。非特异性肺部疾病患者无阳性反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[SENSITIVITY OF THE NEW SKIN TEST DIASKINTEST® FOR THE DIAGNOSIS OF TUBERCULOSIS INFECTION IN CHILDREN AND ADOLESCENTS].

In Russia, an intradermal Diaskintest® drug has been designed, which is a recombinant tuberculosis allergen based on M. tuberculosis-- specific proteins: ESAT-6 and CFP-10 produced by a genetically modified Escherichia coli culture. Diaskintest® test and Mantoux test with 2TE PPD-L were concurrently carried out in 300 children and adolescents with tuberculosis and followed up in risk groups at a tuberculosis dispensary to determine the sensitivity of the new skin test in active tuberculosis infection. Diaskintest® showed a high sensitivity not only in active tuberculosis, but also in occult, the so-called latent, tuberculosis infection. This is suggested by the following evidence. The high percentage (83.8%) of positive responses to Diaskintest® is noted in children and adolescents with tuberculosis, receiving an intensive course of chemotherapy. Negative tests were observed only in minor forms at the resolution stage. In the children who had completed treatment, positive tests were seen in 78.3%, moreover in those with prior tuberculosis of intrathoracic lymph nodes; negative tests were observed not earlier than 18 months after start of treatment. The highest sensitivity of Diaskintest® was shown in children with early primary tuberculosis infection and through family contact with bacteria-excreting subjects (91.7%). These children may be judged with the highest assurance to have latent tuberculosis infection, the population of which is in an active state at the moment of the study. The children with early primary tuberculosis infection, but in no family contact with bacteria-excreting individuals, showed a lower percentage of positive responses to Diaskintest® both before (37.5%) and after (10%) treatment, which suggests that there must be a lower bacterial burden in the child. A high percentage of positive responses to Diaskintest® (76.2%) were found in subjects with hyperergic reactions to tuberculin. These were in only 16.7% in the group of patients receiving preventive therapy. In children and adolescents with a persistent positive Mantoux test (for more than 3 years), the response to Diaskintest® was negative in most cases since in early infection when mycobacteria propagated, the reaction to the drug was positive, but as 3 years pass the probability of the infection transition to the persistence stage is high--at that time the response to Diaskintest® becomes negative. Diaskintest® induces no delayed hypersensitivity associated with BCG vaccination, suggesting its high specificity. There were no positive reactions in patients with nonspecific lung diseases.

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